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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 5 (DOID:0110575)
Synonyms: autosomal dominant deafness 5; DFNA5
Alt IDs: OMIM:600994, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life and high frequency progressive hearing loss and has_material_basis_in mutation in the DFNA5 gene on chromosome 7p15.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/23/2017
MGI 6.09
The Jackson Laboratory